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(E)-1-cyclohexyl-1-octen-3-yne is a unique organic compound characterized by its molecular structure, which consists of a cyclohexyl group attached to an octen-3-yne chain. The "E" notation indicates that the molecule has a trans configuration, meaning the substituents on the double bond are on opposite sides of the molecule. (E)-1-cyclohexyl-1-octen-3-yne is known for its distinct chemical properties and potential applications in various fields, such as pharmaceuticals and materials science. Its structure provides a balance between the stability of the cyclohexyl ring and the reactivity of the alkyne group, making it an interesting subject for chemical research and synthesis.

51760-71-5

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51760-71-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51760-71-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,7,6 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 51760-71:
(7*5)+(6*1)+(5*7)+(4*6)+(3*0)+(2*7)+(1*1)=115
115 % 10 = 5
So 51760-71-5 is a valid CAS Registry Number.

51760-71-5Downstream Products

51760-71-5Relevant academic research and scientific papers

HIGHLY STEREOSELECTIVE SYNTHESES OF CONJUGATED E,E- AND E,Z-DIENES, E-ENYNES AND E-1,2,3-BUTATRIENES VIA ALKENYLBORANE DERIVATIVES

Negishi, Ei-ichi,Yoshida, Takao,Abramovitch, Akiva,Lew, George,Williams, Robert M.

, p. 343 - 356 (2007/10/02)

A highly selective and potentially general methodology for the synthesis of conjugated E,E- and E,Z-dienes, E-enynes, and E-1,2,3-butatrienes via hydroboration of alkynes is reported.The observed stereoselectivity was >98-99percent.

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